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About the Role

The Quality Control Inspector I will execute Quality Control processes for purchased product, production, supplier quality, and departmental calibration and maintenance. This role involves inspecting purchased parts and assemblies, overseeing instrument calibration, maintaining laboratory supplies, and supporting continuous improvement projects.

Responsibilities

• Execute Quality Control processes for purchased product, production, supplier quality, and departmental calibration and maintenance.
• Inspect purchased parts and assemblies used to manufacture Luminex products.
• Oversee and assure calibration and maintenance of measuring and monitoring instruments.
• Maintain IQC laboratory supplies.
• Maintain the integrity and cleanliness of the QC work area.
• Support continuous process improvement projects and perform cross-functional job duties.
• Communicate supplier quality to internal and external parties.
• Drive continuous improvement projects, including developing department inspection methods and resolving audit observations, non-conformances, corrective actions, and customer complaints.
• Address Supplier Quality issues.
• Perform incoming dimensional inspection of precision machined, molded and electromechanical parts using hand tools.
• Perform inspections with Optical Comparator, Digital Microscope, Profilometer.
• Program and operate Zeiss CMM and vision system using Calypso software.
• Process purchased materials for release.
• Apply GD&T practices.
• Take ownership and assist in core QC functions and associated activities relating to Incoming Product Control.
• Fulfill individual and departmental CAPP objectives.
• Assist and document the investigation and resolution of problems initiated through non-conformances, corrective action, customer complaints, and/or audit findings.
• Coordinate and/or conduct departmental maintenance and calibration of local measuring and monitoring devices.
• Schedule outsourced testing and services.
• Maintain cleanliness and integrity of facilities and working areas.
• Lead and assist with departmental document change control and engineering change control activities.
• Monitor and assess impact of procedural and engineering change releases.
• Lead and assist in development of test methods and inspection plans.
• Assist in Material Review Board activities.
• Lead and assist in continuous improvement projects.
• Conduct applicable departmental and interdepartmental training.
• Interface with other departments and participate in meetings.
• Ensure personal compliance and facilitate department compliance with the Quality System and Health and Safety policies.
• Monitor and stock departmental supplies; generate Purchase Orders as needed.
• Assist in validations of test methods, equipment, processes.
• Drive the resolution of audit findings, observations, and recommendations.
• Participate in additional quality activities as required.
• Drive scheduling of day to day processes; ensure timely and accurate turnaround.
• Liaison with Purchasing for supplier interactions.
• Guide procurement for non-recurring resources.
• Assist in data analysis and reporting of department metrics.
• Assist in the development and improvements of incoming inspection methods, inspection plans, and test fixtures.
• Assist with departmental obligations for product design and development, design transfer, and market phases.
• Perform functional inspection and testing of critical components using spectrophotometers, vision systems, and CMMs.
• Lead in programming of CMM and vision system.
• Perform First Article Inspections of Alpha, Beta and Market Release products.
• Perform First Article Inspections on CMM.
• Coordinate supplier source inspections.
• Assist in resolving Supplier Quality issues with regard to inspection methods.
• Investigate and communicate supplier quality issues / failures.
• Drive supplier resolution in supplier non-conformances.
• Assist in core Final QC functions and associated activities relating to Intermediate and Finished Product Control.
• Process intermediate and finished products for release.
• Document non-conformances.
• Assist in continuous improvement projects.
• Assist in the resolution of audit findings, observations, and recommendations.
• Assist in the investigation and resolution of problems initiated through non-conformances, corrective action, or customer complaints.
• Assist in validations of test methods, equipment, processes.
• Perform other duties as assigned.

Requirements

• HS Diploma or equivalent required.
• Proficient knowledge of secondary finishing processes (i.e., plating, powder coating, polishing etc..).

Skills

• Caliper
• Pin Gauges
• Height Gauge
• Thread Gauges
• Micrometers
• Optical Comparator
• Digital Microscope
• Profilometer
• Zeiss CMM
• Calypso software
• GD&T practices
• Oracle transactions
• Spectrophotometers
• Vision systems
• CMMs

Location

• United States
• Canada

Work Type

• Full-time

Experience Level

• 5 years relevant work experience or training OR 7 years related experience without Associate's degree

Education Level

• HS Diploma or equivalent
• Associate's degree in a technical field preferred

Benefits

• Competitive salary and benefits package

About the Company

• Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide.
• With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.
• Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist."
• When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
• Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
• We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.
• If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.
• Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!

Equal Opportunity

• Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.
• In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.
• Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at hrtalent@diasorin.com or 1-800-328-1482 to request an accommodation.